- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
61 result(s) found for: Free Energy.
Displaying page 1 of 4.
| EudraCT Number: 2014-002720-27 | Sponsor Protocol Number: 2014-002720-27 | Start Date*: 2014-12-04 |
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
| Full Title: Simplification from Tenofovir plus Lamivudine or Emtricitabine plus Ritonavir-Boosted-Protease Inhibitor to Ritonavir-Boosted-Atazanavir plus Lamivudine in Virologically-Suppressed-HIV-Infected Adu... | ||
| Medical condition: Chronic HIV infection. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000238-23 | Sponsor Protocol Number: ExeBAT01 | Start Date*: 2016-08-09 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: The effect of Exenatide on brown adipose tissue activity and energy expenditure in healthy young men | ||
| Medical condition: Healthy volunteers, intended indications: obesity and dyslipidemia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001594-40 | Sponsor Protocol Number: UNOLE0526 | Start Date*: 2016-05-10 | |||||||||||
| Sponsor Name:University of Leicester | |||||||||||||
| Full Title: SGLT-2 Inhibitor Empagliflozin Effects on Appetite and Weight Regulation: A randomised double-blind placebo-controlled trial (SEESAW) | |||||||||||||
| Medical condition: Type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004059-34 | Sponsor Protocol Number: C7Q040 | Start Date*: 2021-02-25 | |||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||
| Full Title: Stimulation of the beta-2 adrenergic receptor for activating human brown adipose tissue | |||||||||||||
| Medical condition: Obesity, overweight, lipid- and glucose metabolism | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000322-19 | Sponsor Protocol Number: UX007-CL202 | Start Date*: 2016-06-06 |
| Sponsor Name:Ultragenyx Pharmaceutial Inc. | ||
| Full Title: An Open-label Long-Term Safety and Efficacy Extension Study in Subjects with Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) Previously Enrolled in UX007 or Triheptanoin Studies | ||
| Medical condition: Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000730-19 | Sponsor Protocol Number: DC2019ROCKIES1 | Start Date*: 2020-03-05 |
| Sponsor Name:Amsterdam Univeristy Medical Center - Vu Univeristy Medical Center | ||
| Full Title: A phase 4, monocenter, prospective, randomized, placebo-controlled, double-blind, cross-over mechanistic intervention trial to assess effect of 4-week Ertugliflozin (SGLT-2 inhibitor) therapy on re... | ||
| Medical condition: Type 2 Diabetes Mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002909-10 | Sponsor Protocol Number: P137 | Start Date*: 2022-10-24 |
| Sponsor Name:Maastricht University | ||
| Full Title: THE IMPACT OF PSILOCYBIN ON PAIN IN FIBROMYALGIA PATIENTS AND HEALTHY VOLUNTEERS: A MULTICENTER TRIAL | ||
| Medical condition: Fibromyalgia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002539-32 | Sponsor Protocol Number: The_WE_Study | Start Date*: 2015-03-23 | |||||||||||
| Sponsor Name:St. Olavs University Hospital | |||||||||||||
| Full Title: The WE Study - Walking Easier with cerebral palsy | |||||||||||||
| Medical condition: cerebral palsy | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) FR (Ongoing) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001063-36 | Sponsor Protocol Number: eNERGY | Start Date*: 2016-06-16 | |||||||||||
| Sponsor Name:CHU Rennes | |||||||||||||
| Full Title: Randomised phase III study testing nivolumab versus chemotherapy in first line treatment of PS 2 or elderly (more than 70 years old) patients with advanced non-small cell lung cancer | |||||||||||||
| Medical condition: Advanced non small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004122-18 | Sponsor Protocol Number: 2012GR12 | Start Date*: 2014-12-12 | |||||||||||
| Sponsor Name:University of Dundee, Tayside Clinical Trials Unit | |||||||||||||
| Full Title: A Prospective Study to Evaluate the Effect of Allopurinol on Muscle Energetics in Older People with Impaired Physical Function. | |||||||||||||
| Medical condition: FUNCTIONAL IMPAIRMENT | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000825-35 | Sponsor Protocol Number: U1111-1167-2731 | Start Date*: 2015-08-27 | |||||||||||
| Sponsor Name:Rigshospitalet Blegdamsvej | |||||||||||||
| Full Title: The effect of the glucagon-like peptide-1 analogue, liraglutide (Victoza®), on jejunostomy output and intestinal absorption in short bowel syndrome patients, a double-blind cross-over study | |||||||||||||
| Medical condition: Short bowel syndrome (SBS) is a clinical situation with reduced absorptive mucosal surface due to extensive surgical resection. SBS leads to increased intestinal losses of fluids and electrolytes; ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001779-22 | Sponsor Protocol Number: 04.2017 | Start Date*: 2017-07-10 | |||||||||||
| Sponsor Name:Aarhus University Hospital, Department of Endocrinology | |||||||||||||
| Full Title: The Effect of Empagliflozin on Cardiac and Kidney Metabolism in Persons with Type 2 Diabetes | |||||||||||||
| Medical condition: Diabetes, type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004149-26 | Sponsor Protocol Number: METRIS-HF(EMPA) | Start Date*: 2018-06-26 |
| Sponsor Name:Charité Universitätsmedizin Berlin | ||
| Full Title: Effect of Metformin and Empagliflozin in insulin resistant patients with heart failure with reduced ejection fraction | ||
| Medical condition: Heart Failure with reduced ejection fraction (HFrEF and HFmrEF) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001452-30 | Sponsor Protocol Number: 010815testis | Start Date*: 2015-12-07 | |||||||||||
| Sponsor Name:Copenhagen University Hospital Rigshospitalet | |||||||||||||
| Full Title: A Randomized double-blind study of testosterone replacement therapy or placebo in testicular cancer survivors with mild Leydig Cell Insufficiency (Einstein-intervention) | |||||||||||||
| Medical condition: Leydig Cell dysfunction | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000237-48 | Sponsor Protocol Number: MiraBAT01 | Start Date*: 2016-04-20 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: The effect of Mirabegron on brown adipose tissue in healthy young white Caucasian and South Asian men | ||
| Medical condition: Obesity and dyslipidemia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003532-39 | Sponsor Protocol Number: SitaBAT01 | Start Date*: 2014-11-24 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: The effect of sitagliptin on brown adipose tissue and whole-body metabolism in overweight pre-diabetic men | ||
| Medical condition: Obesity, dyslipidemia and impaired glucose tolerance | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000604-25 | Sponsor Protocol Number: R96-A6604-14-S22 | Start Date*: 2015-05-02 |
| Sponsor Name:Danish Cancer Society Research Center | ||
| Full Title: HBOT LYCA: Hyperbaric Oxygen Therapy to reduce Lymphoedema after Breast Cancer - an explorative clinical trial | ||
| Medical condition: breast cancer related lymphedema | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001559-30 | Sponsor Protocol Number: SMKV-013-CP4 | Start Date*: 2017-09-13 | |||||||||||
| Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
| Full Title: Efficacy of long-term parenteral nutrition with SmofKabiven® E concomitant to chemo- and/or immunotherapy: A prospective, randomised, controlled, open, multicentre, two-stage, adaptive clinical tri... | |||||||||||||
| Medical condition: Metastatic Non-Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002721-99 | Sponsor Protocol Number: CT114-2022-01 | Start Date*: 2023-03-28 | |||||||||||
| Sponsor Name:Klinikum Nürnberg | |||||||||||||
| Full Title: Natriuretic-ureothelic adaptation of body fluid homeostasis during SGLT-2 inhibition and/or mineralocorticoid receptor modulation in patients with chronic kidney disease. A 4-arm, double-blind, dou... | |||||||||||||
| Medical condition: Stage 3 chronic kidney disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002693-35 | Sponsor Protocol Number: B3D-EW-GHDK | Start Date*: 2008-11-21 | |||||||||||
| Sponsor Name:Eli Lilly and Company Ltd | |||||||||||||
| Full Title: Comparison of the Effects of Teriparatide with those of Risedronate on Lumbar Spine Bone Mineral Density in Men and Postmenopausal Women with Low Bone Mass and a Recent Pertrochanteric Hip Fracture | |||||||||||||
| Medical condition: Postmenopausal Women and Men with Low Bone Mass and a Recent Pertrochanteric Fracture | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) GR (Completed) SE (Completed) AT (Completed) FR (Completed) CZ (Completed) IE (Completed) FI (Completed) NO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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